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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400224생성일: 2026년 10월 26일

2-Hydroxyisobutyric acid → 2-hydroxy-2-methyl-propionic acid(S)-2-[(1R,3aR,4S,7aR)-4-(tert-butyl-dimethyl-silanyloxy)-7a-methyl-octahydro-inden-1-yl]-propyl ester

https://huagongshe.com/reaction/400224

반응식

참여 물질

역할이름HCID투입량
반응물2-Hydroxyisobutyric acidHCID 11671—
반응물TriphenylphosphineHCID 11776—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propan-1-olHCID 15230899—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-hydroxy-2-methyl-propionic acid(S)-2-[(1R,3aR,4S,7aR)-4-(tert-butyl-dimethyl-silanyloxy)-7a-methyl-octahydro-inden-1-yl]-propyl esterHCID 1866635491%

반응 조건

온도0 °C

반응 단계

200 mg (0,612 mmol) of (S)-2-[(1R,3aR,4S,7aR)-4-(tert-butyl-dimethyl-silanyloxy)-7a-methyl-octahydro-inden-1-yl]-propan-1-ol was dissolved in THF (2 ml). PPh3 (169 mg; 0,643 mmol) was added and the mixture cooled to 0° C. To this, a solution of DEAD (95 mg; 0,612 mmol) and 2-hydroxy-isobutyric acid (64 mg; 0,612 mmol) in THF (2 ml) was added dropwise via cannula. After four hours the reaction mixture was poured in cold water, extracted with ether and dried over Na2SO4. Removal of the solvent and silica gel column chromatography (eluent hexane/ethyl-acetate 85/15) of the residue afforded 232 mg (91%) of 2-hydroxy-2-methyl-propionic acid(S)-2-[(1R,3aR,4S,7aR)-4-(tert-butyl-dimethyl-silanyloxy)-7a-methyl-octahydro-inden-1-yl]-propyl ester (K1) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05827883
출처 데이터셋uspto-grants-1998_10
ORD IDord-7c1d61e2cebd4a67bc256db3185810d7
출처 메모uspto-grants-1998_10